Senior Clinical Manager

Title : Global Clinical Operations Manager

Location : Remote anywhere in Germany (with travel)

Contact : [email protected]

The company

Here is a rare and great opportunity to join an international manufacturer in surgical devices and be part of this company’s new digitalized Clinical & Medical Affairs processes.

You will be reporting directly to their global headquarters to a Senior Director in Germany.

This exciting position will give you the opportunity to work in an international, English speaking environment and work closely with internal German, USA, Canadian, Asia-Pacific and European teams - including : Sales & Marketing, R&D, Product Management, Regulatory Affairs, Quality Assurance, Risk Management teams.

The Opportunity

Are you a seasoned professional in the medical device industry, ready to take on a new challenge and make a real impact? We're seeking an ambitious and experienced Global Clinical Operations Manager to lead the transformation and digitalization of clinical trials.

If you're passionate about ensuring participant safety, driving operational excellence, and advancing innovative clinical research, we want to hear from you.

Your responsibilities :

• Create strategies & lead the digital transformation of our global clinical operations processes, driving efficiency and excellence
• Build up internal infrastructure globally to enable the company to run internal clinical trials and investigations
• Initiate pragmatic and efficient clinical research & investigation processes
• Influence cross-functional and cross-cultural teams to adopt new ideas, SOPs, and systems globally
• Procure, review and control the implementation of new digital clinical tools
• Promote and foster a patient-centric and data-driven mindset across the organization, driving innovation and impact

Your qualifications :

• Minimum 5 years of experience in designing, planning & implementing clinical SOPs and systems for internal clinical operations from industry environments
• Experience in planning & implementing clinical studies in the EU and the US (project management, creating protocols and study documents, sit management, monitoring, audit, reporting, vendor management)
• Proven GCP / EN ISO 14155 certification or similar training
• Fluent English language (verbal and written)

If you are interested in this exciting role, please send your application directly to [email protected]

Please note : Due to the high volume of applications we sometimes receive, our team might not be able to contact each applicant individually regarding the status of their application.

If you do not hear from us after 10 days, please consider your application unsuccessful.